Jan H. Veldink focuses on Amyotrophic lateral sclerosis, Genetics, Genome-wide association study, Single-nucleotide polymorphism and Disease. The study incorporates disciplines such as SNP, Neuroscience and Mutation in addition to Amyotrophic lateral sclerosis. Allele, Gene, Expression quantitative trait loci, Gene expression profiling and Haplotype are the primary areas of interest in his Genetics study.
His Genome-wide association study research includes themes of Quantitative trait locus, Genetic architecture, Genetic association, Locus and Genetic variation. His study looks at the relationship between Single-nucleotide polymorphism and fields such as Phenotype, as well as how they intersect with chemical problems. His Disease study integrates concerns from other disciplines, such as Endocrinology and Subclinical infection.
The scientist’s investigation covers issues in Amyotrophic lateral sclerosis, Genetics, Genome-wide association study, Internal medicine and Disease. Pathology covers Jan H. Veldink research in Amyotrophic lateral sclerosis. His Pathology research incorporates elements of Neuroscience and Spinal cord.
Single-nucleotide polymorphism, Gene, Locus, Allele and Genetic variation are among the areas of Genetics where the researcher is concentrating his efforts. Jan H. Veldink works mostly in the field of Genome-wide association study, limiting it down to topics relating to Genetic association and, in certain cases, Genetic architecture, as a part of the same area of interest. His Internal medicine research incorporates themes from Gastroenterology, Endocrinology, Surgery and Oncology.
Amyotrophic lateral sclerosis, Genetics, Genome-wide association study, Gene and Computational biology are his primary areas of study. Jan H. Veldink has included themes like C9orf72, Case-control study and Genetic association in his Amyotrophic lateral sclerosis study. Genome-wide association study is a subfield of Single-nucleotide polymorphism that Jan H. Veldink tackles.
His study focuses on the intersection of Single-nucleotide polymorphism and fields such as Frontotemporal dementia with connections in the field of Neuropsychology and Audiology. His studies deal with areas such as Genome, Short read, Sequencing data, Microsatellite and Locus as well as Computational biology. The Internal medicine study combines topics in areas such as Gastroenterology and Oncology.
His scientific interests lie mostly in Amyotrophic lateral sclerosis, Genetics, Computational biology, Genome-wide association study and Genome. His research integrates issues of Biomarker, Survival analysis and Case-control study in his study of Amyotrophic lateral sclerosis. His work in Gene, Genetic association, Mutation, Allele and Phenotype is related to Genetics.
Jan H. Veldink has researched Genetic association in several fields, including Quantitative trait locus, Expression quantitative trait loci and Genomics. Genome-wide association study is a primary field of his research addressed under Single-nucleotide polymorphism. His work in the fields of Single-nucleotide polymorphism, such as Linkage disequilibrium, overlaps with other areas such as Human leukocyte antigen.
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Genome-wide association study identifies five new schizophrenia loci
Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau.
Nature Genetics (2016)
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra;Marjolein J Peters;Tõnu Esko;Hanieh Yaghootkar.
Nature Genetics (2013)
Multiple common variants for celiac disease influencing immune gene expression
Patrick C. A. Dubois;Gosia Trynka;Lude Franke;Lude Franke;Karen A. Hunt.
Nature Genetics (2010)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli;Brittany N Lasseigne;Slave Petrovski;Peter C Sapp.
Science (2015)
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C. Francioli;Androniki Menelaou;Sara L. Pulit;Freerk van Dijk.
Nature Genetics (2014)
Controversies and priorities in amyotrophic lateral sclerosis
Martin R Turner;Orla Hardiman;Michael Benatar;Benjamin R Brooks.
Lancet Neurology (2013)
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Wouter van Rheenen;Aleksey Shatunov;Annelot M. Dekker;Russell L. McLaughlin.
Nature Genetics (2016)
Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA.
Rudolf S. N. Fehrmann;Ritsert C. Jansen;Jan H. Veldink;Harm-Jan Westra.
PLOS Genetics (2011)
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Aude Nicolas;Kevin P. Kenna;Alan E. Renton;Alan E. Renton;Nicola Ticozzi.
Neuron (2018)
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